Variant report

Variant	rs550919167
Chromosome Location	chr4:100888391-100888392
allele	C/G
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	esv3397740	chr4:100887913-100888396	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100880400-100889600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:100882600-100889000	Weak transcription	Osteobl	bone
3	chr4:100882800-100888400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr4:100882800-100892800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr4:100883000-100889000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:100887000-100890000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:100887200-100888400	Enhancers	NHLF	lung
8	chr4:100887400-100888400	Enhancers	Dnd41	blood
9	chr4:100887800-100889800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:100887800-100890200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:100888000-100888800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr4:100888200-100888400	Weak transcription	Muscle Satellite Cultured Cells	--

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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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