Variant report

Variant	rs7904582
Chromosome Location	chr10:118557321-118557322
allele	A/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	chr10:118556200-118557400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:118556200-118557400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
3	chr10:118556400-118562800	Weak transcription	Brain Germinal Matrix	brain
4	chr10:118557200-118557400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:118557200-118557400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:118557200-118557400	Flanking Active TSS	Fetal Heart	heart

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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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