Variant report

Variant	rs8024385
Chromosome Location	chr15:34300989-34300990
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:34299066..34301596-chr15:34326883..34329699,2	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1872806	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2078561	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2078562	0.91[CEU][hapmap];0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2243858	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2632075	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2632076	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2632078	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2632079	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2632107	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2684931	1.00[CEU][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2684932	0.96[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2684933	0.84[EUR][1000 genomes]
rs2684953	0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2684956	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2684958	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2702278	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2702284	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2702285	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28471985	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28870091	0.96[ASN][1000 genomes]
rs525591	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs544114	0.95[ASN][1000 genomes]
rs602807	0.87[CHB][hapmap];0.84[ASN][1000 genomes]
rs603152	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs604041	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs61611317	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs635531	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs644585	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs646950	0.91[CHB][hapmap];0.82[ASN][1000 genomes]
rs6495448	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6495459	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7177293	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs718690	0.84[EUR][1000 genomes]
rs8035125	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8035294	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8039574	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8039609	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9806210	1.00[EUR][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	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv903985	chr15:34279319-34370487	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34265400-34311800	Weak transcription	Liver	Liver
2	chr15:34274400-34311000	Weak transcription	Primary B cells from cord blood	blood
3	chr15:34277800-34303200	Weak transcription	Gastric	stomach
4	chr15:34278200-34310000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:34281000-34306800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:34283000-34306000	Weak transcription	Ovary	ovary
7	chr15:34289400-34303800	Weak transcription	Psoas Muscle	Psoas
8	chr15:34292000-34315000	Weak transcription	Aorta	Aorta
9	chr15:34294800-34315600	Weak transcription	Left Ventricle	heart
10	chr15:34295400-34304000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr15:34297000-34306800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr15:34300400-34303200	Weak transcription	HSMM	muscle

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