Variant report

Variant	rs376449088
Chromosome Location	chrX:76709220-76709221
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	nsv531129	chrX:76703995-77038914	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 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	chrX:76705000-76710600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chrX:76705000-76713800	Weak transcription	Primary hematopoietic stem cells	blood
3	chrX:76705600-76710800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chrX:76706200-76710800	Weak transcription	Fetal Muscle Trunk	muscle
5	chrX:76707200-76711000	Weak transcription	HUVEC	blood vessel
6	chrX:76708000-76710600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chrX:76708800-76709600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chrX:76709200-76709400	Enhancers	Fetal Muscle Leg	muscle
9	chrX:76709200-76710600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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