Variant report

Variant	rs36047004
Chromosome Location	chr3:111780067-111780068
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111772600-111780200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:111779800-111780600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr3:111779800-111780600	Enhancers	Placenta Amnion	Placenta Amnion
4	chr3:111779800-111780800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:111779800-111780800	Enhancers	NH-A	brain
6	chr3:111779800-111780800	Enhancers	Osteobl	bone
7	chr3:111780000-111780600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:111780000-111780600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:111780000-111780600	Enhancers	Fetal Kidney	kidney
10	chr3:111780000-111780800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:111780000-111780800	Enhancers	A549	lung

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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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