Variant report

Variant	rs7650400
Chromosome Location	chr3:102439536-102439537
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	chr3:102436503..102438389-chr3:102438528..102440294,2	MCF-7	breast:

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

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

rs_ID	r²[population]
rs11708911	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11720453	0.98[ASN][1000 genomes]
rs12486666	0.85[ASN][1000 genomes]
rs12495176	0.86[ASN][1000 genomes]
rs1354727	0.95[ASN][1000 genomes]
rs1391422	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1391423	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1474186	0.95[ASN][1000 genomes]
rs1498081	0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1498086	0.85[ASN][1000 genomes]
rs1506436	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1581303	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1581304	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1589287	0.98[ASN][1000 genomes]
rs1599776	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1609976	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1715542	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1715546	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1715547	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1715553	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1715554	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17831612	0.89[EUR][1000 genomes]
rs2088475	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2971239	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34116120	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4241417	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4383531	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4856111	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4856112	0.97[ASN][1000 genomes]
rs4856130	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4856149	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55635554	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6441670	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6441671	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6764453	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6768201	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6768503	0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6770963	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73137703	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73137731	0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73137742	0.89[EUR][1000 genomes]
rs73139703	0.89[EUR][1000 genomes]
rs73139709	0.89[EUR][1000 genomes]
rs7355983	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7636527	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7639003	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9290744	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs939326	0.95[ASN][1000 genomes]
rs9810913	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9844846	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007340	chr3:102108954-102725099	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv536676	chr3:102108954-102725099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1009392	chr3:102199756-102631205	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv877228	chr3:102345638-102751470	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv591190	chr3:102345638-102946216	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv834776	chr3:102351486-102532042	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1000584	chr3:102358773-102923378	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
8	nsv915978	chr3:102386795-102949530	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv877229	chr3:102415127-102649650	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr3:102436800-102440600	Weak transcription	Fetal Heart	heart

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