Variant report

Variant	rs3802910
Chromosome Location	chr11:121772755-121772756
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:121767400-121773000	Weak transcription	NHDF-Ad	bronchial
2	chr11:121767400-121775600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:121767400-121775600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:121769200-121776200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr11:121770000-121777800	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr11:121770400-121772800	Weak transcription	NHLF	lung
7	chr11:121771600-121774400	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr11:121772600-121775800	Weak transcription	NHEK	skin

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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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