Variant report

Variant	rs377289745
Chromosome Location	chr18:8670602-8670603
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3450483	chr18:8670052-8673550	Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:8653800-8703400	Weak transcription	Right Atrium	heart
2	chr18:8662200-8673400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr18:8663400-8671800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr18:8667000-8672800	Weak transcription	A549	lung
5	chr18:8668600-8671800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr18:8668800-8673000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr18:8669600-8672200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr18:8669600-8674000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr18:8669800-8671800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr18:8670600-8671000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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