Variant report

Variant	rs569338380
Chromosome Location	chr8:60830608-60830609
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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3376604	chr8:60830385-60830715	Weak transcription Enhancers	n/a	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	chr8:60828400-60832200	Weak transcription	Colon Smooth Muscle	Colon
2	chr8:60828600-60834800	Weak transcription	Fetal Stomach	stomach
3	chr8:60828800-60834000	Weak transcription	Stomach Smooth Muscle	stomach
4	chr8:60830000-60831200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr8:60830000-60834000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr8:60830000-60834200	Enhancers	Primary B cells from peripheral blood	blood
7	chr8:60830200-60833600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:60830400-60831600	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr8:60830600-60831800	Weak transcription	GM12878-XiMat	blood

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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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