Variant report

Variant	rs61636440
Chromosome Location	chr14:78666289-78666290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10129486	1.00[EUR][1000 genomes]
rs10133423	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10137760	1.00[EUR][1000 genomes]
rs10141650	0.89[AFR][1000 genomes]
rs10151566	1.00[AMR][1000 genomes]
rs11850806	0.89[AFR][1000 genomes]
rs74063974	1.00[AMR][1000 genomes];1.00[EUR][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	nsv1366	chr14:78633044-78677718	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78662800-78667800	Weak transcription	Brain Angular Gyrus	brain
2	chr14:78665000-78678000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:78665400-78670000	Enhancers	Fetal Thymus	thymus
4	chr14:78665800-78667800	Enhancers	Brain Germinal Matrix	brain
5	chr14:78666000-78666400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr14:78666000-78666800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:78666000-78666800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:78666000-78670200	Enhancers	Thymus	Thymus

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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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