Variant report

Variant	rs12452760
Chromosome Location	chr17:66624741-66624742
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11077688	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11656342	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12452734	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12940313	0.91[EUR][1000 genomes]
rs2024166	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2907385	1.00[CHB][hapmap]
rs8071496	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8077820	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9675199	1.00[CHB][hapmap]
rs9890441	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv833524	chr17:66524030-66705194	Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv908693	chr17:66619054-66647840	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66623600-66624800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr17:66623800-66625200	Enhancers	Fetal Kidney	kidney
3	chr17:66624000-66624800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr17:66624000-66625000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr17:66624000-66625000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr17:66624000-66625000	Enhancers	HMEC	breast
7	chr17:66624200-66624800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr17:66624200-66624800	Enhancers	HSMMtube	muscle
9	chr17:66624200-66625000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr17:66624200-66625000	Enhancers	HSMM	muscle
11	chr17:66624200-66625000	Enhancers	Osteobl	bone
12	chr17:66624400-66624800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr17:66624600-66624800	Enhancers	Rectal Smooth Muscle	rectum
14	chr17:66624600-66625800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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Input of quick search could be:

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

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