Variant report

Variant	rs7149326
Chromosome Location	chr14:78670583-78670584
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10129486	1.00[ASN][1000 genomes]
rs10137760	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10138043	1.00[JPT][hapmap]
rs10145155	1.00[ASN][1000 genomes]
rs28610490	1.00[ASN][1000 genomes]
rs28622289	1.00[ASN][1000 genomes]
rs56948116	1.00[ASN][1000 genomes]
rs57816474	1.00[ASN][1000 genomes]
rs73322235	1.00[ASN][1000 genomes]
rs73322257	1.00[ASN][1000 genomes]
rs73322263	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	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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78665000-78678000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:78668400-78670600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:78668600-78670600	Enhancers	NHEK	skin
4	chr14:78669400-78672000	Weak transcription	Brain Germinal Matrix	brain
5	chr14:78669800-78675000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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