Variant report

Variant	rs7905131
Chromosome Location	chr10:117642123-117642124
allele	C/T
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	chr10:117634000-117657800	Weak transcription	Aorta	Aorta
2	chr10:117636800-117644000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr10:117639800-117642600	Weak transcription	Fetal Stomach	stomach
4	chr10:117641200-117642200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr10:117641600-117642200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr10:117641600-117642200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr10:117641600-117642400	Bivalent Enhancer	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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