Variant report

Variant	rs76885347
Chromosome Location	chr4:20406073-20406074
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	esv1004503	chr4:20399974-20409944	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3420991	chr4:20405954-20410452	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20393200-20408800	Weak transcription	Colon Smooth Muscle	Colon
2	chr4:20404200-20406200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:20404600-20406200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:20405000-20406400	Enhancers	Brain Anterior Caudate	brain
5	chr4:20405200-20419600	Weak transcription	NHDF-Ad	bronchial
6	chr4:20405400-20406200	Enhancers	Brain Hippocampus Middle	brain
7	chr4:20405600-20406200	Enhancers	Brain Substantia Nigra	brain
8	chr4:20405800-20406200	Enhancers	Fetal Lung	lung
9	chr4:20406000-20409200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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