Variant report

Variant	rs537678360
Chromosome Location	chr10:18630802-18630803
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046458	chr10:18629603-18683860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18629400-18631600	Active TSS	Left Ventricle	heart
2	chr10:18629400-18632600	Active TSS	Right Atrium	heart
3	chr10:18629400-18632800	Active TSS	Right Ventricle	heart
4	chr10:18629600-18633000	Active TSS	Fetal Heart	heart
5	chr10:18630000-18633800	Weak transcription	Liver	Liver
6	chr10:18630000-18639200	Weak transcription	Pancreas	Pancrea
7	chr10:18630200-18639200	Weak transcription	Ovary	ovary
8	chr10:18630400-18631000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr10:18630400-18632200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:18630600-18631000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	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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