Variant report

Variant	rs56198873
Chromosome Location	chr11:15541739-15541740
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15541000-15542000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr11:15541200-15541800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr11:15541400-15541800	Enhancers	H1 Cell Line	embryonic stem cell
4	chr11:15541400-15541800	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr11:15541400-15541800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr11:15541600-15541800	Enhancers	Esophagus	oesophagus

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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