Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11915975	1.00[MEX][hapmap]
rs11925864	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs16825048	1.00[CHB][hapmap]
rs16825099	1.00[CHB][hapmap]
rs16825113	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs16825235	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16825341	0.81[LWK][hapmap];0.90[YRI][hapmap];0.85[AFR][1000 genomes]
rs17349490	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs2320186	1.00[CHB][hapmap]
rs359571	1.00[CHD][hapmap]
rs57296021	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58819809	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61493707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66459918	0.85[AFR][1000 genomes]
rs73007057	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73007059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73007060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7630469	1.00[CHB][hapmap];1.00[CHD][hapmap]
rs7645934	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs934591	1.00[CHB][hapmap]

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	nsv1009618	chr3:155370034-155492177	Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:155383400-155393800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:155383400-155394000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:155383400-155395800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr3:155383600-155394000	Weak transcription	Pancreas	Pancrea
5	chr3:155385200-155394000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr3:155390600-155393800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr3:155390800-155393200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr3:155391800-155393800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:155391800-155393800	Weak transcription	Fetal Intestine Small	intestine
10	chr3:155391800-155394000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr3:155392400-155393800	Weak transcription	Fetal Intestine Large	intestine
12	chr3:155392800-155394600	Active TSS	Right Atrium	heart
13	chr3:155393000-155393200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:155393000-155393400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr3:155393000-155394000	Weak transcription	HepG2	liver
16	chr3:155393000-155394400	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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