Variant report

Variant	rs531002470
Chromosome Location	chr5:94324413-94324414
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756469	chr5:94323268-94400017	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94301200-94337600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:94313800-94337000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr5:94314000-94325400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:94319800-94346600	Weak transcription	HUVEC	blood vessel
5	chr5:94320400-94348000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr5:94322400-94334200	Weak transcription	Gastric	stomach
7	chr5:94323200-94326200	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr5:94323800-94325800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr5:94324000-94324600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr5:94324400-94326000	Strong transcription	Primary monocytes fromperipheralblood	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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