Variant report

Variant	rs532625290
Chromosome Location	chr14:70951806-70951807
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv565042	chr14:70951234-71011734	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	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	chr14:70910600-70955600	Weak transcription	Left Ventricle	heart
2	chr14:70948000-70955000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr14:70949000-70956000	Weak transcription	Primary T helper cells PMA-I stimulated	--
4	chr14:70949200-70956400	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr14:70949400-70956200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr14:70951200-70956200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr14:70951400-70955000	Weak transcription	Aorta	Aorta
8	chr14:70951400-70957600	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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