Variant report

Variant	rs2746137
Chromosome Location	chr6:69428801-69428802
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:69426489..69429415-chr6:69449508..69452167,3	K562	blood:
2	chr6:69423760..69426080-chr6:69427890..69430012,2	K562	blood:
3	chr6:69427276..69429730-chr6:69482240..69484850,2	K562	blood:
4	chr6:69428185..69430149-chr6:69436142..69437737,2	K562	blood:
5	chr6:69423520..69425895-chr6:69426993..69429775,2	K562	blood:
6	chr6:69348325..69348840-chr6:69428482..69429102,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1033520	0.83[JPT][hapmap]
rs10455674	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10455676	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10484791	0.95[CHB][hapmap];0.94[JPT][hapmap];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10945138	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10945139	0.95[CHB][hapmap];0.94[JPT][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10945141	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs10945142	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs11752398	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11752837	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12154008	0.95[CHB][hapmap];0.95[JPT][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12192235	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12199251	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12200101	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12201488	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12206940	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12210045	1.00[CHB][hapmap];0.88[JPT][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12214149	0.84[CHB][hapmap];0.88[JPT][hapmap]
rs13218712	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2073135	0.83[JPT][hapmap];0.87[ASN][1000 genomes]
rs2246104	0.90[CHB][hapmap];0.94[JPT][hapmap]
rs2253759	0.88[JPT][hapmap];0.86[EUR][1000 genomes]
rs2253866	0.89[JPT][hapmap];0.95[EUR][1000 genomes]
rs2254654	1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2585592	0.84[JPT][hapmap];0.88[EUR][1000 genomes]
rs2585597	0.84[JPT][hapmap];0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2585598	0.83[JPT][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2585599	0.90[JPT][hapmap];0.84[AFR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2585600	0.90[JPT][hapmap];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2585604	0.90[JPT][hapmap];0.85[AFR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2585621	1.00[CHB][hapmap];0.94[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2585622	1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2585623	0.95[EUR][1000 genomes]
rs2746125	0.89[JPT][hapmap];0.84[AFR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2746127	0.84[JPT][hapmap];0.85[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs2746130	0.85[AFR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2746131	0.83[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2746132	0.89[JPT][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2746134	0.85[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2746135	0.91[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2746140	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2746141	0.83[JPT][hapmap];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2802676	0.95[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2802677	0.91[AFR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2802680	0.90[JPT][hapmap];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2802683	0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2802684	0.89[JPT][hapmap];0.86[AFR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2802687	0.84[JPT][hapmap];0.88[EUR][1000 genomes]
rs2802688	0.84[JPT][hapmap];0.85[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs2802689	0.88[JPT][hapmap]
rs2802691	0.83[JPT][hapmap];0.86[EUR][1000 genomes]
rs2802693	0.88[JPT][hapmap]
rs2802694	0.84[JPT][hapmap]
rs2802701	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs3121775	0.84[JPT][hapmap];0.87[EUR][1000 genomes]
rs41328149	0.83[JPT][hapmap]
rs4358587	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4507548	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6931354	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs715294	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7745837	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7768591	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][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	nsv886130	chr6:68950298-69531957	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv970728	chr6:69426786-69430815	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 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	chr6:69421400-69436400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:69427800-69430200	Enhancers	Fetal Heart	heart
3	chr6:69428000-69429000	Enhancers	Brain Cingulate Gyrus	brain
4	chr6:69428000-69430000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:69428200-69429000	Enhancers	Brain Angular Gyrus	brain
6	chr6:69428200-69429000	Enhancers	Fetal Lung	lung
7	chr6:69428200-69429400	Enhancers	Brain Germinal Matrix	brain
8	chr6:69428400-69429000	Enhancers	NH-A	brain
9	chr6:69428400-69429200	Enhancers	Fetal Brain Male	brain
10	chr6:69428600-69429000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:69428600-69429000	Enhancers	Brain Substantia Nigra	brain
12	chr6:69428600-69429000	Enhancers	Fetal Brain Female	brain
13	chr6:69428600-69429200	Flanking Active TSS	NHDF-Ad	bronchial
14	chr6:69428800-69429000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:69428800-69429000	Enhancers	K562	blood
16	chr6:69428800-69435000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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