Variant report

Variant	rs28612937
Chromosome Location	chr2:210404305-210404306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:210392000-210406000	Weak transcription	Fetal Brain Female	brain
2	chr2:210392400-210405400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:210393400-210405400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr2:210397000-210406800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:210399000-210405600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:210401400-210405200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:210402600-210405400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr2:210404000-210407000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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