Variant report

Variant	rs113584899
Chromosome Location	chr3:50711164-50711165
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	esv3398465	chr3:50710948-50713996	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50687000-50712000	Weak transcription	Right Atrium	heart
2	chr3:50708800-50711400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:50709000-50711400	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:50709000-50711600	Weak transcription	Pancreas	Pancrea
5	chr3:50709000-50711600	Weak transcription	Right Ventricle	heart
6	chr3:50709000-50711800	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:50709000-50711800	Weak transcription	Esophagus	oesophagus
8	chr3:50709200-50711400	Weak transcription	Brain Angular Gyrus	brain
9	chr3:50709400-50711800	Weak transcription	HSMMtube	muscle
10	chr3:50710200-50711800	Weak transcription	HSMM	muscle
11	chr3:50711000-50711600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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