Variant report

Variant	rs7030762
Chromosome Location	chr9:102166506-102166507
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:102165899..102167637-chr9:102167880..102169522,2	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10441761	0.83[EUR][1000 genomes]
rs10760684	0.80[EUR][1000 genomes]
rs10760685	0.80[EUR][1000 genomes]
rs10819661	0.83[EUR][1000 genomes]
rs10819666	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10819667	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10819672	0.84[EUR][1000 genomes]
rs10819674	0.80[EUR][1000 genomes]
rs10988816	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10988829	0.80[EUR][1000 genomes]
rs12238127	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2416768	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4743345	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4743347	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4743348	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4743349	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4743353	0.80[EUR][1000 genomes]
rs55750347	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs57483311	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7027953	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7032399	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7032541	0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7040144	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73495500	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7857445	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7858078	0.83[EUR][1000 genomes]
rs878449	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs880597	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893620	chr9:102029791-102194921	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv831667	chr9:102068047-102285691	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102162800-102169000	Weak transcription	Fetal Heart	heart
2	chr9:102163000-102169000	Weak transcription	Right Ventricle	heart
3	chr9:102166400-102169000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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