Variant report

Variant	rs181781783
Chromosome Location	chr7:127117156-127117157
allele	A/G
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	esv33524	chr7:127116966-127117190	Enhancers Weak transcription	lncRNA	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	chr7:127111000-127125000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:127116000-127117200	Enhancers	Pancreas	Pancrea
3	chr7:127116400-127117600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:127116400-127117800	Weak transcription	Gastric	stomach
5	chr7:127116400-127118200	Enhancers	Stomach Mucosa	stomach
6	chr7:127117000-127117200	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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