Variant report

Variant	rs7832079
Chromosome Location	chr8:131694284-131694285
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	chr17:59938342..59941056-chr8:131692920..131695356,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136492	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10088420	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10095393	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10095479	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10095628	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10095820	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10096321	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10098463	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10101790	0.87[CEU][hapmap];0.89[JPT][hapmap]
rs10107223	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10108730	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10112041	0.89[ASN][1000 genomes]
rs10113164	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11985368	0.84[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs11993977	0.81[EUR][1000 genomes]
rs11995981	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1509847	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16893283	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16893288	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16904337	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs16904339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1912271	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1912272	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1961665	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28379502	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28428945	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28430960	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28870411	0.85[EUR][1000 genomes]
rs4294201	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4472534	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4483174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4560808	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59406705	0.85[EUR][1000 genomes]
rs7002882	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7004166	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs715679	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72728275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72728278	0.90[ASN][1000 genomes]
rs72728285	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73344752	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7822131	0.88[EUR][1000 genomes]
rs7831277	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7844774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs952132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs956481	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][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	nsv533085	chr8:131042781-131755007	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv915864	chr8:131509799-131754822	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2752684	chr8:131641096-131710094	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv612294	chr8:131645079-131923377	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv891448	chr8:131668278-131968469	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131686200-131694800	Weak transcription	Esophagus	oesophagus
2	chr8:131688200-131694800	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr8:131688400-131694400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr8:131688400-131694400	Weak transcription	HSMMtube	muscle
5	chr8:131688400-131694600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr8:131688400-131694600	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr8:131688600-131694400	Weak transcription	NHDF-Ad	bronchial
8	chr8:131689800-131694400	Weak transcription	HMEC	breast
9	chr8:131690200-131694400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:131690200-131694600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:131691400-131694400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr8:131692200-131694400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:131692400-131694400	Weak transcription	K562	blood
14	chr8:131692800-131696400	Weak transcription	Brain Germinal Matrix	brain
15	chr8:131693400-131694400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:131693400-131694400	Enhancers	A549	lung
17	chr8:131693400-131696600	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr8:131693600-131694400	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr8:131693600-131694400	Enhancers	NHLF	lung
20	chr8:131694000-131694400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:131694000-131704400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr8:131694200-131694400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:131694200-131694400	Enhancers	Fetal Muscle Trunk	muscle
24	chr8:131694200-131694400	Weak transcription	Ovary	ovary
25	chr8:131694200-131694400	Enhancers	NHEK	skin
26	chr8:131694200-131694600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr8:131694200-131694600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr8:131694200-131694600	Enhancers	Hela-S3	cervix
29	chr8:131694200-131694800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr8:131694200-131695200	Enhancers	Fetal Muscle Leg	muscle
31	chr8:131694200-131695400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links