Variant report

Variant	rs57328745
Chromosome Location	chr3:160304408-160304409
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	chr3:160284666..160286841-chr3:160302799..160304775,2	MCF-7	breast:
2	chr3:160298872..160300468-chr3:160304100..160306105,2	K562	blood:

Variant related genes	Relation type
ENSG00000229320	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10513550	0.83[ASN][1000 genomes]
rs2305401	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2305406	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs33999879	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3736627	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3773371	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3806629	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41272959	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56124988	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56343019	1.00[ASN][1000 genomes]
rs56396435	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56401539	0.84[EUR][1000 genomes]
rs57030267	0.83[ASN][1000 genomes]
rs57050097	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57277659	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs57555307	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58377812	0.91[ASN][1000 genomes]
rs58654032	0.83[ASN][1000 genomes]
rs58776572	0.84[EUR][1000 genomes]
rs58915028	0.83[ASN][1000 genomes]
rs59695030	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59799252	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs60066272	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60153357	0.83[ASN][1000 genomes]
rs60517889	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs60607858	0.84[EUR][1000 genomes]
rs61066536	0.83[ASN][1000 genomes]
rs62272193	0.83[ASN][1000 genomes]
rs62272196	0.83[ASN][1000 genomes]
rs62272197	0.83[ASN][1000 genomes]
rs62272198	0.83[ASN][1000 genomes]
rs62272231	0.83[ASN][1000 genomes]
rs62272236	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62272237	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62272245	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62272247	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62272249	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62272251	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62272254	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272255	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272256	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272257	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272258	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272259	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62272780	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272781	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272783	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272785	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272787	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272788	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272790	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272793	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62272799	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62272804	1.00[ASN][1000 genomes]
rs62272805	1.00[ASN][1000 genomes]
rs62272806	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272831	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272833	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272836	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62272838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66769612	0.83[ASN][1000 genomes]
rs66850724	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67403526	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs68069205	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73154587	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73155914	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7645798	0.80[EUR][1000 genomes]
rs7648832	0.87[EUR][1000 genomes];0.95[ASN][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	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1000453	chr3:159853305-160366357	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
3	nsv536779	chr3:159853305-160366357	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
4	nsv877702	chr3:160262803-160304614	Flanking Active TSS Active TSS Weak transcription Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
5	nsv4089	chr3:160284848-160330024	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160299000-160305000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:160304000-160306000	Enhancers	Skeletal Muscle Female	skeletal muscle

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