Variant report

Variant	rs10090835
Chromosome Location	chr8:130789767-130789768
allele	A/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]
rs1600794	1.00[ASW][hapmap]
rs4733559	1.00[ASW][hapmap]
rs62524565	0.83[AMR][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	nsv428524	chr8:130731660-130894467	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130780400-130790200	Weak transcription	Spleen	Spleen
2	chr8:130780400-130797000	Weak transcription	Esophagus	oesophagus
3	chr8:130785400-130790600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr8:130787200-130790200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:130787200-130790400	Strong transcription	NHEK	skin
6	chr8:130789000-130791400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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