Variant report

Variant	rs11186557
Chromosome Location	chr10:93164257-93164258
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93162400-93168800	Weak transcription	HSMM	muscle
2	chr10:93162800-93169000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:93163000-93164400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr10:93163000-93164600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr10:93163000-93164600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr10:93163000-93166000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr10:93163000-93167600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr10:93163000-93168400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr10:93163000-93168800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr10:93163600-93168400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr10:93164200-93164600	Bivalent Enhancer	Fetal Brain Male	brain
12	chr10:93164200-93164800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr10:93164200-93165000	Enhancers	H9 Derived Neuron 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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