Variant report

Variant	rs17132748
Chromosome Location	chr10:4412650-4412651
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11813500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11815971	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11817023	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11818101	1.00[AMR][1000 genomes]
rs11819442	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1616155	1.00[AMR][1000 genomes]
rs1679412	1.00[AMR][1000 genomes]
rs1679432	1.00[AMR][1000 genomes]
rs17132623	1.00[AMR][1000 genomes]
rs17132691	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17132695	1.00[AMR][1000 genomes]
rs17132779	1.00[AMR][1000 genomes]
rs1751278	1.00[AMR][1000 genomes]
rs1751281	1.00[AMR][1000 genomes]
rs1751294	1.00[AMR][1000 genomes]
rs74111157	1.00[AMR][1000 genomes]
rs74111159	1.00[AMR][1000 genomes]
rs7899030	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv894786	chr10:4385379-4441989	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv894787	chr10:4385379-4857717	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4411600-4413200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr10:4411800-4413800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:4412000-4412800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr10:4412000-4414200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr10:4412200-4413000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr10:4412400-4412800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:4412600-4412800	Enhancers	Skeletal Muscle Female	skeletal muscle
8	chr10:4412600-4412800	Weak transcription	NHDF-Ad	bronchial
9	chr10:4412600-4413000	Enhancers	Primary hematopoietic stem cells	blood
10	chr10:4412600-4413000	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr10:4412600-4413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr10:4412600-4413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:4412600-4413000	Enhancers	Fetal Kidney	kidney
14	chr10:4412600-4413000	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr10:4412600-4413200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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