Variant report

Variant	rs533540951
Chromosome Location	chr11:23561347-23561348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832087	chr11:23404474-23569183	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1038101	chr11:23556680-23685548	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23561000-23561400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr11:23561000-23561600	Enhancers	Dnd41	blood
3	chr11:23561000-23562600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:23561000-23563200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:23561200-23561400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:23561200-23561400	Enhancers	Aorta	Aorta
7	chr11:23561200-23561400	Enhancers	Colon Smooth Muscle	Colon
8	chr11:23561200-23561600	Enhancers	Fetal Intestine Large	intestine
9	chr11:23561200-23561600	Enhancers	NHLF	lung
10	chr11:23561200-23561800	Enhancers	Stomach Mucosa	stomach
11	chr11:23561200-23561800	Enhancers	NH-A	brain
12	chr11:23561200-23562200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr11:23561200-23562200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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