Variant report

Variant	rs16866767
Chromosome Location	chr2:180399670-180399671
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180394000-180401200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr2:180397000-180401000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:180397800-180403600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:180398400-180402800	Weak transcription	Liver	Liver
5	chr2:180399400-180399800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:180399600-180402200	Weak transcription	Psoas Muscle	Psoas

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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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