Variant report

Variant	rs58281777
Chromosome Location	chr4:20427853-20427854
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20420800-20433400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr4:20421000-20433600	Weak transcription	Aorta	Aorta
3	chr4:20421200-20430400	Weak transcription	NHLF	lung
4	chr4:20421200-20431800	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:20421400-20433400	Weak transcription	Brain Anterior Caudate	brain
6	chr4:20422400-20429600	Weak transcription	Brain Substantia Nigra	brain
7	chr4:20423600-20428600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr4:20423600-20431800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:20424800-20428200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:20424800-20429000	Weak transcription	NHDF-Ad	bronchial
11	chr4:20424800-20431800	Weak transcription	Osteobl	bone
12	chr4:20425600-20431200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr4:20427200-20432200	Weak transcription	Hela-S3	cervix
14	chr4:20427400-20428000	Enhancers	Colon Smooth Muscle	Colon
15	chr4:20427600-20428000	Enhancers	Brain Hippocampus Middle	brain
16	chr4:20427600-20428800	Enhancers	Fetal Lung	lung
17	chr4:20427600-20432400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:20427800-20428000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

Quick Search:

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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