Variant report

Variant	rs9483576
Chromosome Location	chr6:133663743-133663744
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133654600-133667800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:133660400-133664000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:133661400-133663800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:133662200-133679200	Weak transcription	Psoas Muscle	Psoas
5	chr6:133662400-133664600	Enhancers	Hela-S3	cervix
6	chr6:133663000-133663800	Enhancers	Gastric	stomach
7	chr6:133663200-133667400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:133663400-133664400	Enhancers	A549	lung
9	chr6:133663400-133666600	Weak transcription	hESC Derived CD184+ Endoderm 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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