Variant report

Variant	rs2655829
Chromosome Location	chr2:167625197-167625198
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs2664012	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6721470	0.94[EUR][1000 genomes]

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	nsv529384	chr2:167143465-167958752	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875375	chr2:167515013-167703912	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:167622800-167629800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr2:167623000-167628000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:167623200-167628200	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr2:167623600-167628000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:167624000-167628000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr2:167624000-167628200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr2:167624000-167628200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:167624600-167625200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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