Variant report

Variant	rs7152477
Chromosome Location	chr14:78622984-78622985
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs59588653	1.00[EUR][1000 genomes]
rs732176	1.00[EUR][1000 genomes]
rs73316336	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	nsv902109	chr14:78603877-78634174	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78619200-78623800	Weak transcription	Brain Hippocampus Middle	brain
2	chr14:78619800-78623400	Weak transcription	Brain Germinal Matrix	brain
3	chr14:78622200-78623000	Enhancers	NHEK	skin
4	chr14:78622400-78623000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr14:78622800-78623000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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