Variant report

Variant	rs576172450
Chromosome Location	chr6:82320238-82320239
allele	A/G
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	nsv604087	chr6:81792413-82326091	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv517168	chr6:82319174-82325529	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82317600-82323000	Weak transcription	NHLF	lung
2	chr6:82318000-82323000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:82318000-82323000	Weak transcription	NH-A	brain
4	chr6:82318000-82323000	Weak transcription	NHDF-Ad	bronchial
5	chr6:82318000-82323200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:82318000-82356600	Weak transcription	Aorta	Aorta
7	chr6:82318200-82323000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr6:82318800-82322800	Weak transcription	Osteobl	bone
9	chr6:82318800-82323000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:82318800-82323000	Weak transcription	HUVEC	blood vessel

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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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