Variant report

Variant	rs77619585
Chromosome Location	chr8:122846275-122846276
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3346096	chr8:122846191-122846615	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv1339710	chr8:122846275-122846279	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv389772	chr8:122846276-122846279	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122843000-122848400	Enhancers	Fetal Lung	lung
2	chr8:122844200-122853800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:122844600-122846800	Enhancers	Fetal Intestine Large	intestine
4	chr8:122846200-122847600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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