Variant report

Variant	rs9556440
Chromosome Location	chr13:95574018-95574019
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs942913	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]

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	nsv832687	chr13:95412811-95582161	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95572000-95574400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:95572000-95574400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr13:95572000-95574400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr13:95572000-95574400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr13:95572200-95574200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr13:95572200-95574200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr13:95572600-95574200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr13:95573600-95574200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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