Variant report

Variant	rs35120800
Chromosome Location	chr14:84492026-84492027
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:6)

rs_ID	r²[population]
rs12879560	1.00[ASN][1000 genomes]
rs12879625	1.00[ASN][1000 genomes]
rs12883081	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12886515	1.00[ASN][1000 genomes]
rs12887005	1.00[ASN][1000 genomes]
rs17656234	1.00[ASN][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	nsv1382	chr14:84487547-84532237	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84489800-84493800	Weak transcription	Fetal Stomach	stomach
2	chr14:84491000-84493200	Weak transcription	Ovary	ovary
3	chr14:84491800-84492200	Enhancers	H9 Cell Line	embryonic stem cell
4	chr14:84491800-84492200	Enhancers	Fetal Lung	lung
5	chr14:84491800-84492200	Enhancers	Pancreas	Pancrea
6	chr14:84492000-84492200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:84492000-84492200	Enhancers	Adipose Nuclei	Adipose
8	chr14:84492000-84492400	Enhancers	Right Atrium	heart

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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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