Variant report

Variant	rs577636774
Chromosome Location	chr5:151293089-151293090
allele	A/G
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	nsv531994	chr5:151292664-151331097	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151291600-151293200	Enhancers	Aorta	Aorta
2	chr5:151291800-151293600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:151292000-151293200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr5:151292000-151294600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:151292200-151293200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
6	chr5:151292600-151293200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
7	chr5:151292600-151293400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:151292800-151297200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr5:151293000-151293400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell

Quick Search:

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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