Variant report

Variant	rs10136794
Chromosome Location	chr14:55732663-55732664
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3396352	chr14:55731649-55734247	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv85138	chr14:55732654-55732673	Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv84632	chr14:55732654-55732675	Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv85479	chr14:55732663-55732673	Weak transcription	Chromatin interactive region	2 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	chr14:55730200-55733000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:55730600-55735000	Weak transcription	HSMMtube	muscle
3	chr14:55730600-55737400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr14:55730800-55733400	Weak transcription	Fetal Heart	heart
5	chr14:55732600-55737400	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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