Variant report

Variant	rs185104120
Chromosome Location	chr2:125728254-125728255
allele	C/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	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
3	esv3429891	chr2:125727632-125729830	Enhancers Active TSS Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
4	esv3356161	chr2:125728082-125729380	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125726400-125729400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr2:125728000-125732800	Weak transcription	Brain Anterior Caudate	brain
3	chr2:125728200-125728400	Enhancers	Brain Cingulate Gyrus	brain
4	chr2:125728200-125729000	Enhancers	Brain Inferior Temporal Lobe	brain
5	chr2:125728200-125732600	Weak transcription	Brain Hippocampus Middle	brain
6	chr2:125728200-125732600	Weak transcription	Brain Substantia Nigra	brain

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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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