Variant report

Variant	rs532520733
Chromosome Location	chr18:44815134-44815135
allele	G/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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44810400-44819200	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr18:44813400-44815400	Weak transcription	Pancreas	Pancrea
3	chr18:44814200-44815200	Enhancers	Brain Cingulate Gyrus	brain
4	chr18:44814200-44815600	Bivalent Enhancer	Brain Germinal Matrix	brain
5	chr18:44814400-44815200	Bivalent Enhancer	Fetal Brain Female	brain
6	chr18:44814800-44815200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr18:44814800-44815200	Bivalent Enhancer	Fetal Brain Male	brain
8	chr18:44814800-44815400	Enhancers	Brain Hippocampus Middle	brain
9	chr18:44815000-44815200	Enhancers	HepG2	liver

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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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