Variant report

Variant	rs3860913
Chromosome Location	chr9:86002120-86002121
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:85997879..86001519-chr9:86002024..86006738,6	MCF-7	breast:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10117284	0.82[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs10125072	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10125561	0.80[EUR][1000 genomes]
rs11140060	0.93[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12349789	0.82[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs13299648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs28585601	0.98[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3849865	0.95[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860902	0.81[CEU][hapmap]
rs3860905	0.95[CEU][hapmap];0.84[CHB][hapmap];0.96[JPT][hapmap];0.95[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860906	0.95[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860907	0.95[AFR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860909	0.95[CEU][hapmap];0.83[CHB][hapmap];0.96[JPT][hapmap];0.97[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3860912	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3860914	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3904187	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs3904189	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4297106	0.81[CEU][hapmap];0.86[EUR][1000 genomes]
rs4478644	0.89[CEU][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4877757	0.95[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.94[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7019165	0.93[AFR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7037795	0.97[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7037928	0.98[AFR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85958200-86007600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:85998800-86004200	Weak transcription	Left Ventricle	heart
3	chr9:85998800-86008600	Weak transcription	Pancreas	Pancrea
4	chr9:85999400-86008400	Weak transcription	Aorta	Aorta
5	chr9:86000000-86005800	Weak transcription	Fetal Muscle Leg	muscle
6	chr9:86000000-86006600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr9:86000000-86020600	Weak transcription	Fetal Brain Female	brain
8	chr9:86000400-86005600	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr9:86001000-86002800	Enhancers	HepG2	liver
10	chr9:86001200-86004400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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