Variant report

Variant	rs7818952
Chromosome Location	chr8:11672899-11672900
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11663266..11668513-chr8:11668832..11673585,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000079459	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10089520	1.00[ASN][1000 genomes]
rs10098874	0.92[EUR][1000 genomes]
rs1047643	0.84[EUR][1000 genomes]
rs1138666	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12543666	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17814360	0.82[AMR][1000 genomes]
rs1803250	0.84[AMR][1000 genomes]
rs2409834	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3088244	0.87[AMR][1000 genomes]
rs34809309	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4442098	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55756391	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57720356	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57725348	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60856203	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6984049	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6993946	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7008523	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7009163	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7009514	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7011491	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7013950	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73547720	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73549728	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73549729	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7818816	1.00[ASN][1000 genomes]
rs7843716	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7845566	0.83[EUR][1000 genomes]
rs883034	0.83[EUR][1000 genomes]
rs9644689	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1018978	chr8:11438267-11858466	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv917963	chr8:11540723-11751798	Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1027378	chr8:11541739-11858466	Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	nsv1028229	chr8:11575762-11805961	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv539475	chr8:11575762-11805961	Flanking Active TSS Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv428514	chr8:11580381-11765706	Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv1034014	chr8:11602337-11858466	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv1023803	chr8:11623570-11721655	Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
10	nsv539476	chr8:11623570-11721655	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv890361	chr8:11625808-11755513	Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
12	nsv890362	chr8:11625808-11771089	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1032739	chr8:11643803-11716473	Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv890363	chr8:11647941-11681825	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv1034132	chr8:11657033-12198242	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
16	nsv890365	chr8:11666451-11735641	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	nsv890366	chr8:11666451-11900847	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv1031158	chr8:11666558-11759064	Bivalent Enhancer Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv539477	chr8:11666558-11759064	Enhancers Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
20	nsv1018042	chr8:11667496-11882385	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
21	nsv890367	chr8:11668153-11793529	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
22	nsv890368	chr8:11671041-11718528	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
23	nsv890369	chr8:11671041-11840011	Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11666800-11673000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr8:11666800-11673600	Strong transcription	Fetal Thymus	thymus
3	chr8:11667000-11673000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr8:11667000-11711000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr8:11667200-11673000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr8:11667200-11673400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr8:11667200-11683800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:11667400-11679200	Weak transcription	Fetal Brain Male	brain
9	chr8:11668000-11673400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:11668200-11677800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr8:11669400-11708000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:11669600-11675600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr8:11669600-11678000	Weak transcription	NH-A	brain
14	chr8:11670000-11676000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr8:11670000-11677600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:11670000-11677600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr8:11670000-11677600	Weak transcription	Aorta	Aorta
18	chr8:11670000-11677600	Weak transcription	Fetal Lung	lung
19	chr8:11670000-11677600	Weak transcription	Gastric	stomach
20	chr8:11670000-11677600	Weak transcription	Left Ventricle	heart
21	chr8:11670000-11677600	Weak transcription	Lung	lung
22	chr8:11670000-11678000	Weak transcription	Right Atrium	heart
23	chr8:11670000-11689200	Weak transcription	Fetal Heart	heart
24	chr8:11670400-11675200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:11670400-11677000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr8:11670600-11677400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr8:11670600-11677400	Weak transcription	Esophagus	oesophagus
28	chr8:11670600-11677400	Weak transcription	Fetal Stomach	stomach
29	chr8:11670600-11677800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr8:11670800-11673400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
31	chr8:11670800-11676000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr8:11670800-11677400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:11670800-11677600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:11671000-11679000	Weak transcription	Fetal Kidney	kidney
35	chr8:11671200-11674800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr8:11671200-11678000	Weak transcription	Hela-S3	cervix
37	chr8:11671400-11674200	Weak transcription	Brain Substantia Nigra	brain
38	chr8:11671400-11674400	Strong transcription	HUES6 Cell Line	embryonic stem cell
39	chr8:11671400-11677600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr8:11671400-11677600	Weak transcription	Colonic Mucosa	Colon
41	chr8:11671400-11677600	Weak transcription	Pancreas	Pancrea
42	chr8:11671400-11677600	Weak transcription	Spleen	Spleen
43	chr8:11671400-11677800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr8:11671400-11678000	Weak transcription	Rectal Smooth Muscle	rectum
45	chr8:11671400-11701400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr8:11671600-11673600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr8:11671600-11675800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:11671600-11676000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr8:11671600-11676600	Weak transcription	Small Intestine	intestine
50	chr8:11671600-11677200	Weak transcription	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links