Variant report

Variant	rs4748884
Chromosome Location	chr10:23711120-23711121
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:12)

rs_ID	r²[population]
rs11013460	0.91[EUR][1000 genomes]
rs11013463	0.91[EUR][1000 genomes]
rs12244387	0.91[EUR][1000 genomes]
rs12247204	0.80[ASN][1000 genomes]
rs12251183	0.91[EUR][1000 genomes]
rs4748883	0.82[ASN][1000 genomes]
rs58360574	0.91[EUR][1000 genomes]
rs6482273	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6482274	0.91[EUR][1000 genomes]
rs7070600	0.91[EUR][1000 genomes]
rs7909628	0.82[ASN][1000 genomes]
rs9988767	0.92[EUR][1000 genomes];0.96[ASN][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	nsv825305	chr10:23698620-23740919	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	6 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	chr10:23707000-23711200	Weak transcription	Placenta	Placenta
2	chr10:23709000-23712200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr10:23709400-23711200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:23709400-23712000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:23709800-23712000	Enhancers	Stomach Mucosa	stomach
6	chr10:23710800-23711400	Enhancers	NHEK	skin
7	chr10:23711000-23711200	Enhancers	HMEC	breast
8	chr10:23711000-23711400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr10:23711000-23711400	Flanking Active TSS	Hela-S3	cervix

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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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