Variant report

Variant	rs57894857
Chromosome Location	chr12:117081368-117081369
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117069600-117083600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:117074200-117084000	Weak transcription	Gastric	stomach
3	chr12:117074400-117083000	Weak transcription	Placenta	Placenta
4	chr12:117078000-117085800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr12:117078400-117084200	Weak transcription	Pancreas	Pancrea
6	chr12:117078400-117085600	Weak transcription	Thymus	Thymus
7	chr12:117079600-117081400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr12:117079600-117081800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr12:117079600-117082200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:117080000-117081400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:117080000-117081600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr12:117080600-117082200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr12:117080600-117088000	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr12:117080600-117088000	Weak transcription	Adipose Nuclei	Adipose
15	chr12:117080800-117083800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr12:117081000-117083600	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:117081200-117085400	Weak transcription	Dnd41	blood

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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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