Variant report

Variant	rs11991834
Chromosome Location	chr8:49847305-49847306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1372062	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16938989	1.00[CEU][hapmap]
rs57726830	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66482613	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72640569	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72640576	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72640585	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49845400-49848400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:49846400-49847600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
3	chr8:49846400-49847600	Enhancers	HMEC	breast
4	chr8:49846600-49847400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:49846600-49847400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:49846800-49847400	Bivalent Enhancer	HUVEC	blood vessel
7	chr8:49847000-49847400	Bivalent Enhancer	Osteobl	bone

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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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