Variant report

Variant	rs544218449
Chromosome Location	chr5:94288772-94288773
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	esv3405239	chr5:94288771-94290944	Strong transcription ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94272800-94290800	Weak transcription	Lung	lung
2	chr5:94274200-94289800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:94275400-94290600	Weak transcription	Dnd41	blood
4	chr5:94278000-94290600	Weak transcription	GM12878-XiMat	blood
5	chr5:94282000-94289000	Weak transcription	Adipose Nuclei	Adipose
6	chr5:94285800-94289600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:94286000-94289000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr5:94286200-94289200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr5:94287200-94289000	Strong transcription	HUVEC	blood vessel
10	chr5:94287400-94289000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr5:94288000-94289000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr5:94288200-94294600	Weak transcription	Primary neutrophils fromperipheralblood	blood
13	chr5:94288400-94289200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:94288400-94291400	Weak transcription	Primary T cells from cord blood	blood
15	chr5:94288600-94289000	Strong transcription	Primary hematopoietic stem cells	blood
16	chr5:94288600-94296600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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