Variant report

Variant	rs7821029
Chromosome Location	chr8:49481503-49481504
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]
rs10088149	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10094661	1.00[CEU][hapmap]
rs10097926	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs954949	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49470600-49482400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:49477400-49488800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:49477800-49486400	Weak transcription	Ovary	ovary
4	chr8:49478200-49483800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:49478400-49481600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr8:49478800-49483000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr8:49481200-49482000	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr8:49481400-49481800	Enhancers	NHDF-Ad	bronchial
9	chr8:49481400-49482200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:49481400-49482200	Enhancers	Fetal Lung	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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