Variant report

Variant	rs56267676
Chromosome Location	chr3:23093886-23093887
allele	C/T
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:4)

rs_ID	r²[population]
rs10510535	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2359460	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2359461	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4858470	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23089200-23096800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:23090600-23103800	Weak transcription	Aorta	Aorta
3	chr3:23092800-23094000	Enhancers	GM12878-XiMat	blood
4	chr3:23093400-23094000	Enhancers	Stomach Mucosa	stomach

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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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