Variant report

Variant	rs376496186
Chromosome Location	chrX:104157953-104157954
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916408	chrX:103552340-104347979	Bivalent/Poised TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv521379	chrX:104156944-104181145	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104155400-104158000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chrX:104155400-104158200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chrX:104155400-104158200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chrX:104155400-104158200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chrX:104157200-104158400	Enhancers	Fetal Heart	heart
6	chrX:104157800-104158200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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