Variant report

Variant	rs188281791
Chromosome Location	chr4:47060339-47060340
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	nsv537078	chr4:47059778-47137372	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	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	chr4:47053600-47061800	Weak transcription	Brain Angular Gyrus	brain
2	chr4:47054000-47067000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:47054400-47066800	Weak transcription	Brain Hippocampus Middle	brain
4	chr4:47054600-47063600	Weak transcription	Brain Anterior Caudate	brain
5	chr4:47054600-47066800	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr4:47054600-47075600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr4:47059400-47060600	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr4:47059800-47060400	Enhancers	Hela-S3	cervix
9	chr4:47059800-47060600	Enhancers	Fetal Heart	heart

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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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