Variant report

Variant	rs11014258
Chromosome Location	chr10:25130712-25130713
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11014259	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12245230	0.91[AFR][1000 genomes]
rs73606574	0.81[AFR][1000 genomes]
rs73606578	0.81[AFR][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	esv1817326	chr10:25117363-25138323	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25111800-25140000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr10:25115400-25135600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:25123200-25138600	Weak transcription	Fetal Intestine Small	intestine
4	chr10:25124200-25138600	Weak transcription	Fetal Stomach	stomach
5	chr10:25126600-25135400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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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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