Variant report

Variant	rs376319864
Chromosome Location	chr11:76027957-76027958
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	esv989053	chr11:76027846-76039082	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76025400-76029800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:76025800-76028400	Weak transcription	Hela-S3	cervix
3	chr11:76025800-76029200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:76025800-76031200	Weak transcription	Placenta	Placenta
5	chr11:76026000-76028400	Weak transcription	Adipose Nuclei	Adipose
6	chr11:76026200-76029400	Weak transcription	Fetal Lung	lung
7	chr11:76027000-76032800	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr11:76027600-76029200	Enhancers	Liver	Liver
9	chr11:76027800-76028600	Enhancers	HepG2	liver
10	chr11:76027800-76029000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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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