Variant report

Variant	rs4677447
Chromosome Location	chr3:75130806-75130807
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	STAT3	chr3:75130723-75130876	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
NIPA2P2	TF binding region

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10460949	0.84[EUR][1000 genomes]
rs10460950	0.81[EUR][1000 genomes]
rs12054432	0.94[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12486094	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12488229	0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs12492862	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12493085	0.81[EUR][1000 genomes]
rs12494321	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12496883	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12629483	0.85[EUR][1000 genomes]
rs12632116	0.85[EUR][1000 genomes]
rs12636203	0.87[EUR][1000 genomes]
rs12636209	0.87[EUR][1000 genomes]
rs4076688	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4078307	0.84[EUR][1000 genomes]
rs4234198	0.82[EUR][1000 genomes]
rs4356853	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4361306	0.82[EUR][1000 genomes]
rs4635750	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4676991	0.85[EUR][1000 genomes]
rs4676992	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4677449	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4677458	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4677473	0.87[EUR][1000 genomes]
rs4677474	0.87[EUR][1000 genomes]
rs5009222	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57194478	0.87[EUR][1000 genomes]
rs59643911	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs59715156	0.87[EUR][1000 genomes]
rs62258901	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62260995	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62260996	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62261003	0.86[EUR][1000 genomes]
rs62261005	0.82[EUR][1000 genomes]
rs62261006	0.84[EUR][1000 genomes]
rs62261007	0.82[EUR][1000 genomes]
rs62261008	0.84[EUR][1000 genomes]
rs62261009	0.84[EUR][1000 genomes]
rs62261010	0.82[EUR][1000 genomes]
rs6549689	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6549700	0.86[EUR][1000 genomes]
rs6777388	0.87[EUR][1000 genomes]
rs6800028	0.87[EUR][1000 genomes]
rs72628656	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7429585	0.86[EUR][1000 genomes]
rs7429678	0.83[EUR][1000 genomes]
rs7430106	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7431394	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7432426	0.86[EUR][1000 genomes]
rs7648701	0.84[EUR][1000 genomes]
rs7651120	0.82[EUR][1000 genomes]
rs9310311	0.82[ASN][1000 genomes]
rs9810161	0.83[EUR][1000 genomes]
rs9815881	0.82[ASN][1000 genomes]
rs9816018	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9835668	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9845814	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9850353	0.85[EUR][1000 genomes]
rs9865292	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9869924	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9877977	0.82[ASN][1000 genomes]
rs9882460	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529994	chr3:74720752-75471887	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv916594	chr3:74943399-75540161	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
3	esv1851336	chr3:74970564-75280989	ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1005139	chr3:75027834-75168557	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv534344	chr3:75028665-75164716	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv834736	chr3:75083055-75271458	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
7	esv2760746	chr3:75119190-75140739	Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
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