Variant report

Variant	rs17464733
Chromosome Location	chr8:110692841-110692842
allele	A/C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110679800-110695000	Weak transcription	Fetal Intestine Small	intestine
2	chr8:110691200-110693400	Active TSS	Stomach Smooth Muscle	stomach
3	chr8:110691800-110693000	Active TSS	Brain Anterior Caudate	brain
4	chr8:110691800-110693400	Active TSS	Fetal Brain Female	brain
5	chr8:110692200-110693400	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr8:110692400-110693400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr8:110692600-110693400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:110692800-110693000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr8:110692800-110693200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:110692800-110693200	Enhancers	HUES48 Cell Line	embryonic stem cell

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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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