Variant report

Variant	rs139201949
Chromosome Location	chr14:65661570-65661571
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832817	chr14:65637069-65810406	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
2	nsv564932	chr14:65660502-65691545	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr14:65660600-65663000	Enhancers	Primary B cells from peripheral blood	blood
2	chr14:65661000-65661800	Enhancers	Brain Substantia Nigra	brain
3	chr14:65661000-65662200	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr14:65661000-65662600	Enhancers	HepG2	liver
5	chr14:65661200-65661800	Flanking Active TSS	GM12878-XiMat	blood
6	chr14:65661400-65662000	Weak transcription	Brain Anterior Caudate	brain
7	chr14:65661400-65665000	Weak transcription	Fetal Intestine Large	intestine
8	chr14:65661400-65665000	Weak transcription	Fetal Intestine Small	intestine

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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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