Variant report

Variant	rs13142042
Chromosome Location	chr4:190844038-190844039
allele	A/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	chr4:190839000-190847000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
2	chr4:190839600-190845000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
3	chr4:190840600-190846200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
4	chr4:190840800-190847000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:190843000-190844200	Weak transcription	Fetal Heart	heart
6	chr4:190843200-190844200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr4:190844000-190844800	Weak transcription	Aorta	Aorta
8	chr4:190844000-190845000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood

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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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