Variant report

Variant	rs11792588
Chromosome Location	chr9:104129702-104129703
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:104128710..104133912-chr9:104158398..104162224,6	K562	blood:

Variant related genes	Relation type
ENSG00000136897	Chromatin interaction
ENSG00000136870	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10114241	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10120345	0.94[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs11788457	0.91[EUR][1000 genomes]
rs11788495	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11790458	0.91[EUR][1000 genomes]
rs11793356	0.92[EUR][1000 genomes]
rs11793528	0.92[EUR][1000 genomes]
rs11793745	0.92[EUR][1000 genomes]
rs11793951	0.91[EUR][1000 genomes]
rs11795175	0.92[EUR][1000 genomes]
rs12338315	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12350797	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12351725	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1341761	0.91[EUR][1000 genomes]
rs1341762	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16920215	0.91[EUR][1000 genomes]
rs16920222	0.91[EUR][1000 genomes]
rs1935236	0.91[EUR][1000 genomes]
rs1935237	0.91[EUR][1000 genomes]
rs2417252	0.94[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34914973	0.91[EUR][1000 genomes]
rs41274981	0.92[EUR][1000 genomes]
rs41274983	0.92[EUR][1000 genomes]
rs41281027	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55666756	0.92[EUR][1000 genomes]
rs55899105	0.91[EUR][1000 genomes]
rs55995111	0.91[EUR][1000 genomes]
rs56013964	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56218982	0.92[EUR][1000 genomes]
rs56251240	0.92[EUR][1000 genomes]
rs56389202	0.92[EUR][1000 genomes]
rs57802761	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57833016	0.92[EUR][1000 genomes]
rs58497759	0.92[EUR][1000 genomes]
rs59059615	0.91[EUR][1000 genomes]
rs59311341	0.91[EUR][1000 genomes]
rs61040758	0.91[EUR][1000 genomes]
rs7019447	0.91[EUR][1000 genomes]
rs7023266	0.90[EUR][1000 genomes]
rs7023837	0.91[EUR][1000 genomes]
rs7023948	0.91[EUR][1000 genomes]
rs7023972	0.91[EUR][1000 genomes]
rs7024225	0.90[EUR][1000 genomes]
rs7026000	0.91[EUR][1000 genomes]
rs7034047	0.91[EUR][1000 genomes]
rs7039422	0.91[EUR][1000 genomes]
rs7048634	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73656609	0.91[EUR][1000 genomes]
rs73656612	0.91[EUR][1000 genomes]
rs73656616	0.91[EUR][1000 genomes]
rs73656617	0.91[EUR][1000 genomes]
rs73656618	0.91[EUR][1000 genomes]
rs73656619	0.87[EUR][1000 genomes]
rs73656620	0.91[EUR][1000 genomes]
rs73656621	0.91[EUR][1000 genomes]
rs73656622	0.91[EUR][1000 genomes]
rs73656623	0.91[EUR][1000 genomes]
rs73656624	0.91[EUR][1000 genomes]
rs73656625	0.92[EUR][1000 genomes]
rs73656626	0.92[EUR][1000 genomes]
rs73656627	0.92[EUR][1000 genomes]
rs73656628	0.92[EUR][1000 genomes]
rs73656629	0.92[EUR][1000 genomes]
rs73656630	0.92[EUR][1000 genomes]
rs73656631	0.92[EUR][1000 genomes]
rs73656632	0.92[EUR][1000 genomes]
rs73656633	0.92[EUR][1000 genomes]
rs73656635	0.91[EUR][1000 genomes]
rs73656636	0.92[EUR][1000 genomes]
rs73656637	0.92[EUR][1000 genomes]
rs73656638	0.91[EUR][1000 genomes]
rs73656639	0.92[EUR][1000 genomes]
rs73656640	0.92[EUR][1000 genomes]
rs73656642	0.92[EUR][1000 genomes]
rs73656643	0.92[EUR][1000 genomes]
rs73656644	0.92[EUR][1000 genomes]
rs73656645	0.92[EUR][1000 genomes]
rs73656646	0.92[EUR][1000 genomes]
rs73656647	0.92[EUR][1000 genomes]
rs73656648	0.91[EUR][1000 genomes]
rs73656649	0.92[EUR][1000 genomes]
rs73656650	0.92[EUR][1000 genomes]
rs73657933	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7848855	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7849953	0.89[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	nsv1037157	chr9:104045761-104149233	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv3431849	chr9:104129584-104132561	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104117600-104138800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:104117800-104160000	Weak transcription	Pancreas	Pancrea
3	chr9:104128000-104130600	Enhancers	Fetal Intestine Large	intestine
4	chr9:104128600-104131600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr9:104128600-104135600	Genic enhancers	Liver	Liver
6	chr9:104128800-104133600	Enhancers	K562	blood
7	chr9:104129000-104130200	Weak transcription	Stomach Mucosa	stomach
8	chr9:104129000-104131200	Weak transcription	NH-A	brain
9	chr9:104129000-104132000	Enhancers	HepG2	liver
10	chr9:104129000-104132600	Enhancers	A549	lung
11	chr9:104129000-104138200	Weak transcription	HSMMtube	muscle
12	chr9:104129200-104131200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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