Variant report

Variant	rs370286604
Chromosome Location	chr14:69984227-69984228
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	esv3396933	chr14:69906914-70001258	Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv510642	chr14:69983293-70030335	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr14:69982800-69985200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:69983800-69984400	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:69984000-69984400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
4	chr14:69984000-69984400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr14:69984000-69984400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr14:69984200-69984400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:69984200-69984600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr14:69984200-69985200	Enhancers	Fetal Thymus	thymus
9	chr14:69984200-69985600	Weak transcription	H1 Cell Line	embryonic stem cell

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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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