Variant report

Variant	rs73087882
Chromosome Location	chr20:22454648-22454649
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:22452800-22464000	Weak transcription	Gastric	stomach
2	chr20:22453200-22454800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:22454200-22455200	Enhancers	Stomach Mucosa	stomach
4	chr20:22454600-22454800	Bivalent Enhancer	HepG2	liver

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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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