Variant report

Variant	rs10957669
Chromosome Location	chr8:50786066-50786067
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs13254104	0.81[AFR][1000 genomes]
rs4276702	0.81[AFR][1000 genomes]
rs4437664	0.81[AFR][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	esv3353749	chr8:50530807-51139242	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:50783600-50786200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:50783600-50787000	Weak transcription	NH-A	brain
3	chr8:50783800-50786800	Weak transcription	HMEC	breast
4	chr8:50783800-50787000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:50785000-50787000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:50785200-50787800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:50785400-50787600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:50785800-50786200	Enhancers	H1 Cell Line	embryonic stem cell
9	chr8:50786000-50786200	Enhancers	NHDF-Ad	bronchial

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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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