Variant report

Variant	rs62097142
Chromosome Location	chr18:45108454-45108455
allele	C/G
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	chr18:45104200-45108600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr18:45104600-45110600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr18:45104600-45120000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr18:45104800-45108600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr18:45107000-45110800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr18:45108400-45108800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr18:45108400-45109000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr18:45108400-45114000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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