Variant report

Variant	rs9986304
Chromosome Location	chr5:52706361-52706362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10513022	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13360046	1.00[EUR][1000 genomes]
rs1423560	0.88[CHD][hapmap]
rs16881394	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2019033	1.00[EUR][1000 genomes]
rs3797296	0.84[CHD][hapmap]
rs3891316	1.00[EUR][1000 genomes]
rs9292016	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9292018	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv830297	chr5:52492494-52707758	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52703000-52713400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:52703200-52707000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:52703200-52707200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:52703200-52707600	Weak transcription	Aorta	Aorta
5	chr5:52703200-52713400	Weak transcription	NHLF	lung
6	chr5:52703800-52707000	Weak transcription	Osteobl	bone
7	chr5:52704000-52707000	Weak transcription	NHDF-Ad	bronchial
8	chr5:52704000-52707400	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr5:52704000-52707600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr5:52704600-52712000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr5:52705400-52706600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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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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