Variant report

Variant	rs557356682
Chromosome Location	chr6:133692666-133692667
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	esv3451050	chr6:133692259-133695857	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:133690800-133693200	Active TSS	Hela-S3	cervix
3	chr6:133691400-133698000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:133691400-133700200	Weak transcription	Psoas Muscle	Psoas
5	chr6:133691400-133700800	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:133691600-133701200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:133692400-133693000	Enhancers	A549	lung
8	chr6:133692600-133692800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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