Variant report

Variant	rs2077842
Chromosome Location	chr11:105845944-105845945
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105827400-105850200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:105843000-105850200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:105843800-105866400	Weak transcription	Brain Angular Gyrus	brain
4	chr11:105845000-105846000	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr11:105845800-105846400	Enhancers	Muscle Satellite Cultured Cells	--
6	chr11:105845800-105846400	Enhancers	Hela-S3	cervix
7	chr11:105845800-105846400	Enhancers	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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