Variant report

Variant	rs73721872
Chromosome Location	chr6:11886509-11886510
allele	C/G
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	chr6:11884800-11887800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:11885400-11887000	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr6:11886200-11886600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
4	chr6:11886200-11886600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr6:11886200-11887000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:11886200-11887200	Enhancers	HUES64 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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