Variant report

Variant	rs397843283
Chromosome Location	chr6:133693626-133693627
allele	-/TATAAAA
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	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
2	esv1523433	chr6:133693619-133693626	Weak transcription	n/a	n/a	inside rSNPs	diseases
3	nsv349711	chr6:133693620-133693626	Weak transcription	n/a	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	chr6:133684600-133717800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr6:133691400-133698000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr6:133691400-133700200	Weak transcription	Psoas Muscle	Psoas
4	chr6:133691400-133700800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr6:133691600-133701200	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr6:133693200-133695000	Weak transcription	Hela-S3	cervix

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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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