Variant report

Variant	rs35256669
Chromosome Location	chr4:47044393-47044394
allele	-/TG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3395099	chr4:47043545-47045643	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
2	nsv292674	chr4:47044391-47044410	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv2461818	chr4:47044393-47044394	Weak transcription	n/a	n/a	inside rSNPs	diseases
4	nsv281644	chr4:47044393-47044394	Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv2226134	chr4:47044393-47044395	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47036200-47050200	Weak transcription	Brain Anterior Caudate	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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