Variant report

Variant	rs141987663
Chromosome Location	chr18:45100260-45100261
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3316809	chr18:45099773-45100312	Bivalent Enhancer Weak transcription	n/a	n/a	inside rSNPs	diseases
2	esv3316806	chr18:45099829-45100274	Bivalent Enhancer Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3316808	chr18:45099829-45100278	Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45090200-45103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:45098800-45104000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr18:45099000-45103800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr18:45099000-45104000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr18:45100200-45100800	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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