Variant report

Variant	rs9321383
Chromosome Location	chr6:133168014-133168015
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:133132907..133137002-chr6:133163874..133168278,4	MCF-7	breast:
2	chr6:133139605..133142425-chr6:133167716..133170536,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112306	Chromatin interaction
ENSG00000206754	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1124450	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12193918	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12200907	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12206120	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12207260	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1359142	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1408062	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1408063	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1408064	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1965895	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3756968	0.80[EUR][1000 genomes]
rs4448124	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs451165	0.86[ASN][1000 genomes]
rs4897616	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4897617	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4897618	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6569853	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6569854	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6569857	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569858	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6569859	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6925225	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6926217	0.86[ASN][1000 genomes]
rs7452703	0.80[EUR][1000 genomes]
rs755895	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7743635	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7744235	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7744426	0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7749419	0.86[EUR][1000 genomes]
rs7750176	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7751333	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7751359	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7755422	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7756588	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7756801	0.88[ASN][1000 genomes]
rs7759900	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7764152	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7764252	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7764726	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7766944	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7768470	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9321377	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9321380	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9321382	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9373030	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9375924	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9375925	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9402457	0.80[EUR][1000 genomes]
rs9402460	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9402462	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9493450	0.80[EUR][1000 genomes]
rs9493458	0.80[ASN][1000 genomes]
rs9493465	0.81[EUR][1000 genomes]
rs9493470	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9493474	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
3	nsv886676	chr6:133111706-133168582	Flanking Active TSS Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
4	esv1806734	chr6:133125643-133168582	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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