Variant report

Variant	rs375776014
Chromosome Location	chr2:125711365-125711366
allele	A/G
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	nsv834361	chr2:125601081-125810992	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv874991	chr2:125692490-125901811	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125710200-125712200	Enhancers	Brain Hippocampus Middle	brain
2	chr2:125710200-125712200	Enhancers	Brain Substantia Nigra	brain
3	chr2:125710600-125711400	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr2:125710800-125711400	Enhancers	Brain Angular Gyrus	brain
5	chr2:125711000-125711400	Enhancers	Brain Cingulate Gyrus	brain
6	chr2:125711000-125711400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
7	chr2:125711200-125712000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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