Variant report

Variant	rs71057699
Chromosome Location	chr3:25172428-25172429
allele	-/ATA
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	esv3450541	chr3:25168848-25172646	Flanking Active TSS ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases
2	esv2260027	chr3:25172167-25172668	Enhancers Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
3	esv3441811	chr3:25172361-25172548	Enhancers	n/a	n/a	inside rSNPs	diseases
4	nsv237528	chr3:25172420-25172498	Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25171800-25173600	Enhancers	Fetal Stomach	stomach
2	chr3:25172000-25172600	Enhancers	Fetal Lung	lung

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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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