Variant report

Variant	rs7566048
Chromosome Location	chr2:210503386-210503387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10174385	0.92[EUR][1000 genomes]
rs10179315	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10203283	0.85[EUR][1000 genomes]
rs10208961	0.85[EUR][1000 genomes]
rs1039826	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10497931	0.92[EUR][1000 genomes]
rs12694187	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12988159	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13000863	0.92[EUR][1000 genomes]
rs13382265	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13412699	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13423655	0.82[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13432941	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1396778	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1509467	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1509471	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16843236	0.85[EUR][1000 genomes]
rs1828281	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1949041	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1962197	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1967262	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2063292	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2663644	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2663656	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2710476	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28517694	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs60751322	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6435533	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6752060	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7603837	0.85[EUR][1000 genomes]
rs9288411	1.00[EUR][1000 genomes]
rs992991	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754281	chr2:210484777-210543711	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210494800-210517800	Weak transcription	Aorta	Aorta
2	chr2:210496200-210506800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr2:210496200-210507000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:210501000-210517800	Weak transcription	Fetal Brain Female	brain
5	chr2:210501200-210504200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:210501200-210508000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:210501200-210516200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:210501800-210517800	Weak transcription	Brain Germinal Matrix	brain
9	chr2:210502600-210503600	Enhancers	A549	lung
10	chr2:210502600-210504000	Enhancers	HUVEC	blood vessel
11	chr2:210502800-210503600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr2:210502800-210503800	Enhancers	NH-A	brain
13	chr2:210502800-210504000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:210502800-210504600	Enhancers	NHEK	skin
15	chr2:210502800-210506000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:210502800-210506800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr2:210502800-210508000	Enhancers	HMEC	breast
18	chr2:210503000-210503400	Enhancers	Osteobl	bone
19	chr2:210503000-210503600	Enhancers	NHDF-Ad	bronchial
20	chr2:210503000-210504000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:210503000-210507400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:210503000-210508000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:210503000-210508400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr2:210503200-210506600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr2:210503200-210506800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links