Variant report

Variant	rs7135951
Chromosome Location	chr12:47558849-47558850
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:47557715..47560552-chr12:47561242..47563669,2	MCF-7	breast:
2	chr12:47556322..47559512-chr12:47571534..47574931,3	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10785658	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs10785660	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10881056	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10881057	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10881058	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11183755	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs11183769	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11183774	0.89[CEU][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12371765	0.90[CEU][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12578995	0.89[CEU][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1357933	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1357935	1.00[CEU][hapmap];0.85[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1525444	0.90[CEU][hapmap];0.88[EUR][1000 genomes]
rs1880600	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1917658	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1949864	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs4768141	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4768777	0.89[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6582696	0.81[CEU][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7136496	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7295263	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7299627	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7958186	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs7958922	0.82[EUR][1000 genomes]
rs7963822	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs7974123	0.89[EUR][1000 genomes]
rs9634260	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469368	chr12:47374908-47675680	Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv558784	chr12:47374908-47675680	Genic enhancers Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv832399	chr12:47502910-47689601	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv2751100	chr12:47541390-47746157	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:47536000-47578000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr12:47536200-47564200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:47550400-47560000	Weak transcription	Adipose Nuclei	Adipose
4	chr12:47550400-47562200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:47550600-47571800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr12:47550600-47582400	Weak transcription	Aorta	Aorta
7	chr12:47550800-47560000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr12:47550800-47570000	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:47550800-47570200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr12:47551200-47583600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr12:47551400-47567200	Weak transcription	Spleen	Spleen
12	chr12:47554800-47579600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
13	chr12:47555000-47559800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr12:47555000-47565800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr12:47555000-47576400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
16	chr12:47556600-47560000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:47556800-47560200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr12:47556800-47570400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr12:47557000-47559200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:47557000-47559200	Enhancers	NHDF-Ad	bronchial
21	chr12:47557400-47564600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr12:47557600-47559000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr12:47557600-47559400	Strong transcription	Primary T cells from cord blood	blood
24	chr12:47557800-47560400	Enhancers	A549	lung
25	chr12:47557800-47581600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr12:47558000-47559000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr12:47558000-47559000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr12:47558000-47559000	Enhancers	Osteobl	bone
29	chr12:47558200-47559400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
30	chr12:47558200-47560200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr12:47558400-47559000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr12:47558400-47559000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr12:47558400-47559000	Enhancers	Muscle Satellite Cultured Cells	--
34	chr12:47558400-47559000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:47558600-47559600	Weak transcription	Stomach Mucosa	stomach
36	chr12:47558600-47560400	Enhancers	K562	blood
37	chr12:47558600-47561000	Weak transcription	Gastric	stomach
38	chr12:47558600-47580200	Weak transcription	Primary B cells from cord blood	blood
39	chr12:47558800-47559000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:47558800-47559600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr12:47558800-47559800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:47558800-47559800	Weak transcription	Fetal Intestine Large	intestine
43	chr12:47558800-47559800	Weak transcription	Ovary	ovary
44	chr12:47558800-47559800	Weak transcription	Right Atrium	heart
45	chr12:47558800-47560000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr12:47558800-47561200	Weak transcription	Pancreas	Pancrea
47	chr12:47558800-47570000	Weak transcription	Primary T cells fromperipheralblood	blood
48	chr12:47558800-47582200	Weak transcription	NH-A	brain
49	chr12:47558800-47582400	Weak transcription	Lung	lung

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