Variant report

Variant	rs10498720
Chromosome Location	chr6:24353436-24353437
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12660319	1.00[CEU][hapmap]
rs12661981	1.00[CEU][hapmap]
rs12665371	1.00[CEU][hapmap]
rs16889286	1.00[CEU][hapmap]
rs1772254	1.00[CEU][hapmap]
rs2295651	1.00[CEU][hapmap]
rs3761790	1.00[CEU][hapmap]
rs9379648	0.85[MKK][hapmap]

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	nsv1026638	chr6:24347972-24475300	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24339600-24355600	Weak transcription	Pancreas	Pancrea
2	chr6:24341200-24357600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:24345800-24356800	Weak transcription	Fetal Intestine Large	intestine
4	chr6:24346000-24354800	Weak transcription	A549	lung
5	chr6:24347000-24357000	Weak transcription	Fetal Intestine Small	intestine
6	chr6:24353000-24353600	Genic enhancers	HepG2	liver
7	chr6:24353200-24358800	Active TSS	Fetal Kidney	kidney

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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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