Variant report

Variant	rs7708528
Chromosome Location	chr5:15015137-15015138
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	chr5:15014377..15017867-chr5:15019671..15021896,3	MCF-7	breast:
2	chr5:14663710..14667318-chr5:15013208..15015623,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000154124	Chromatin interaction
ENSG00000261360	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11741614	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11750471	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1446041	1.00[ASN][1000 genomes]
rs1502037	1.00[ASN][1000 genomes]
rs1502038	1.00[ASN][1000 genomes]
rs16903773	0.81[EUR][1000 genomes]
rs16903776	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17342417	1.00[ASN][1000 genomes]
rs2455490	1.00[ASN][1000 genomes]
rs251538	1.00[ASN][1000 genomes]
rs2652759	1.00[ASN][1000 genomes]
rs2652761	1.00[ASN][1000 genomes]
rs28287	1.00[ASN][1000 genomes]
rs301080	1.00[ASN][1000 genomes]
rs32440	1.00[ASN][1000 genomes]
rs32445	1.00[ASN][1000 genomes]
rs32451	1.00[ASN][1000 genomes]
rs32452	1.00[ASN][1000 genomes]
rs32453	1.00[ASN][1000 genomes]
rs32454	1.00[ASN][1000 genomes]
rs32455	1.00[ASN][1000 genomes]
rs32456	1.00[ASN][1000 genomes]
rs32463	1.00[ASN][1000 genomes]
rs32464	1.00[ASN][1000 genomes]
rs32466	1.00[ASN][1000 genomes]
rs32467	1.00[ASN][1000 genomes]
rs62356079	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62356080	1.00[ASN][1000 genomes]
rs62356081	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62356082	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6866660	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6867275	0.81[EUR][1000 genomes]
rs6868543	1.00[ASN][1000 genomes]
rs6873180	1.00[ASN][1000 genomes]
rs6888138	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341022	0.94[CEU][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7708423	0.94[CEU][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7727179	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs836147	1.00[ASN][1000 genomes]
rs836148	1.00[ASN][1000 genomes]
rs836149	1.00[ASN][1000 genomes]
rs856751	1.00[ASN][1000 genomes]
rs863162	1.00[ASN][1000 genomes]
rs9686327	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9687484	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv530221	chr5:14859687-15364470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv432717	chr5:14887400-15126500	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1017579	chr5:14888997-15194335	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv461982	chr5:14943456-15044842	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv597262	chr5:14943456-15044842	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv470991	chr5:14949696-15022112	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv524142	chr5:14986700-15018537	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15009400-15015200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:15009400-15020800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:15009800-15021000	Weak transcription	Aorta	Aorta
4	chr5:15013600-15015200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:15013600-15016400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr5:15013600-15016600	Enhancers	Osteobl	bone
7	chr5:15013800-15015200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr5:15013800-15015200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr5:15013800-15015600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr5:15013800-15015600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:15013800-15015600	Enhancers	Liver	Liver
12	chr5:15013800-15015600	Enhancers	NH-A	brain
13	chr5:15013800-15015800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:15013800-15016200	Enhancers	Fetal Heart	heart
15	chr5:15014000-15015200	Weak transcription	Stomach Mucosa	stomach
16	chr5:15014200-15016400	Enhancers	HSMMtube	muscle
17	chr5:15014600-15015200	Enhancers	NHDF-Ad	bronchial
18	chr5:15014800-15015200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr5:15014800-15015200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr5:15014800-15015200	Flanking Active TSS	HepG2	liver
21	chr5:15014800-15015200	Enhancers	NHEK	skin
22	chr5:15014800-15015400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr5:15014800-15015400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr5:15014800-15015400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr5:15014800-15015600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:15014800-15015600	Flanking Active TSS	A549	lung
27	chr5:15014800-15015600	Enhancers	HSMM	muscle
28	chr5:15015000-15015200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr5:15015000-15015200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr5:15015000-15015200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr5:15015000-15015200	Enhancers	HMEC	breast
32	chr5:15015000-15017000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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