Variant report

Variant	rs2792653
Chromosome Location	chr6:54082138-54082139
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10223728	1.00[MEX][hapmap]
rs1150876	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1150879	1.00[EUR][1000 genomes]
rs1150881	1.00[EUR][1000 genomes]
rs1150882	1.00[EUR][1000 genomes]
rs1150883	1.00[EUR][1000 genomes]
rs1150885	1.00[EUR][1000 genomes]
rs11966518	1.00[EUR][1000 genomes]
rs1280853	0.86[LWK][hapmap];1.00[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1280855	1.00[EUR][1000 genomes]
rs1280856	1.00[EUR][1000 genomes]
rs1280858	1.00[EUR][1000 genomes]
rs1280859	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1280860	1.00[EUR][1000 genomes]
rs1280944	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1290258	1.00[EUR][1000 genomes]
rs1298144	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs1298874	1.00[EUR][1000 genomes]
rs1325832	1.00[MEX][hapmap]
rs1340669	1.00[EUR][1000 genomes]
rs1614889	1.00[EUR][1000 genomes]
rs1775795	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2754784	1.00[EUR][1000 genomes]
rs2754785	1.00[AMR][1000 genomes]
rs2754789	1.00[ASW][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs2754791	1.00[EUR][1000 genomes]
rs2754792	1.00[EUR][1000 genomes]
rs2754799	1.00[EUR][1000 genomes]
rs2754800	1.00[EUR][1000 genomes]
rs2754803	1.00[EUR][1000 genomes]
rs2754805	1.00[EUR][1000 genomes]
rs2754806	1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs2754807	1.00[EUR][1000 genomes]
rs2754810	1.00[EUR][1000 genomes]
rs2754811	1.00[EUR][1000 genomes]
rs2792626	1.00[EUR][1000 genomes]
rs2792628	1.00[EUR][1000 genomes]
rs2792632	1.00[EUR][1000 genomes]
rs2792637	1.00[EUR][1000 genomes]
rs2792639	1.00[EUR][1000 genomes]
rs2792640	0.86[LWK][hapmap];0.81[MKK][hapmap];1.00[EUR][1000 genomes]
rs2792642	1.00[EUR][1000 genomes]
rs2792643	1.00[EUR][1000 genomes]
rs2792645	1.00[EUR][1000 genomes]
rs2792647	1.00[EUR][1000 genomes]
rs2792648	1.00[EUR][1000 genomes]
rs2792650	1.00[MEX][hapmap];1.00[TSI][hapmap]
rs2792651	1.00[EUR][1000 genomes]
rs2792652	0.86[LWK][hapmap];1.00[MEX][hapmap]
rs2792654	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs2792658	1.00[EUR][1000 genomes]
rs28878486	1.00[EUR][1000 genomes]
rs484196	1.00[EUR][1000 genomes]
rs494180	1.00[EUR][1000 genomes]
rs519777	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs526232	1.00[EUR][1000 genomes]
rs553883	1.00[EUR][1000 genomes]
rs554826	1.00[EUR][1000 genomes]
rs55881114	1.00[AMR][1000 genomes]
rs56843634	1.00[EUR][1000 genomes]
rs58420646	1.00[AMR][1000 genomes]
rs587260	1.00[EUR][1000 genomes]
rs58779855	1.00[EUR][1000 genomes]
rs59853271	1.00[EUR][1000 genomes]
rs603260	1.00[EUR][1000 genomes]
rs604566	1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs61111674	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs631431	1.00[EUR][1000 genomes]
rs6458981	1.00[EUR][1000 genomes]
rs667378	1.00[EUR][1000 genomes]
rs6910818	1.00[EUR][1000 genomes]
rs695181	1.00[EUR][1000 genomes]
rs73741492	1.00[AMR][1000 genomes]
rs73741495	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv603110	chr6:53885918-54103794	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1017633	chr6:53935336-54118476	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53998000-54099200	Weak transcription	Psoas Muscle	Psoas
2	chr6:54058800-54101000	Weak transcription	Left Ventricle	heart
3	chr6:54070200-54098800	Weak transcription	Fetal Heart	heart
4	chr6:54070400-54095200	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr6:54081000-54083000	Enhancers	Primary T cells from cord blood	blood
6	chr6:54081400-54082800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr6:54081800-54082200	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:54081800-54082200	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:54081800-54082200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr6:54081800-54082400	Enhancers	HUVEC	blood vessel
11	chr6:54082000-54082400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:54082000-54082600	Enhancers	Dnd41	blood

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