Variant report

Variant	rs546260824
Chromosome Location	chr5:94161691-94161692
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	nsv964907	chr5:94161637-94166013	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	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	chr5:94130400-94192400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr5:94134600-94164000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr5:94137600-94170400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:94140200-94163800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:94148000-94164200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:94157000-94168200	Weak transcription	Thymus	Thymus
7	chr5:94160000-94168200	Weak transcription	GM12878-XiMat	blood
8	chr5:94161400-94163800	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:94161600-94162200	Strong transcription	HUVEC	blood vessel
10	chr5:94161600-94163000	Enhancers	Fetal Thymus	thymus

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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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