Variant report

Variant	rs17424561
Chromosome Location	chr7:106669858-106669859
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106664800-106670000	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr7:106665800-106670200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr7:106669200-106670400	Flanking Active TSS	K562	blood
4	chr7:106669400-106670400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:106669400-106670800	Enhancers	Brain Germinal Matrix	brain
6	chr7:106669400-106670800	Enhancers	Fetal Heart	heart
7	chr7:106669600-106670000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:106669600-106670000	Enhancers	Fetal Lung	lung
9	chr7:106669600-106670200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr7:106669600-106670400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:106669600-106670600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr7:106669800-106670200	Enhancers	Fetal Brain Male	brain
13	chr7:106669800-106670400	Enhancers	Fetal Brain Female	brain
14	chr7:106669800-106672400	Weak transcription	Adipose Nuclei	Adipose

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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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