Variant report

Variant	rs17072796
Chromosome Location	chr13:29686682-29686683
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs12873251	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1467578	0.94[CEU][hapmap];0.80[YRI][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1467579	0.94[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1536717	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1536718	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1536719	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1536720	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1575301	0.94[CEU][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1887749	0.86[EUR][1000 genomes]
rs1887751	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1887752	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1927840	1.00[CEU][hapmap];0.87[JPT][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1927842	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1927843	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1927844	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1952421	1.00[CEU][hapmap];0.86[JPT][hapmap];0.87[EUR][1000 genomes]
rs2025972	1.00[CEU][hapmap];0.87[JPT][hapmap];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2077255	0.81[CHB][hapmap]
rs2094557	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2149322	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2182990	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2475529	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2475530	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2475531	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2475532	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2475533	0.94[CEU][hapmap];0.81[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2475534	0.94[CEU][hapmap];0.81[JPT][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2475536	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2475537	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2479789	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2479790	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2479791	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2479792	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2479793	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2479794	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2479795	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2479796	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2479798	0.94[CEU][hapmap];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2479801	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2479803	0.94[CEU][hapmap];0.81[JPT][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2987345	0.94[CEU][hapmap];0.81[JPT][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3751402	0.94[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3829381	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4238115	1.00[CEU][hapmap];0.87[JPT][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6490350	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6490351	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6490352	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6490355	1.00[CEU][hapmap];0.87[JPT][hapmap];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs656803	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs685778	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7324366	0.94[CEU][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7324548	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7326464	0.81[CHB][hapmap]
rs7331544	0.90[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7334488	0.89[CEU][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7336281	0.94[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7337190	0.81[CHB][hapmap]
rs745423	0.80[CHB][hapmap]
rs754395	0.81[CHB][hapmap]
rs7981238	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7981689	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7982710	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7985792	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7986301	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7987444	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7994251	0.94[CEU][hapmap];0.90[JPT][hapmap]
rs7994936	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7995588	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7999357	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7999521	0.89[EUR][1000 genomes]
rs913494	0.81[CHB][hapmap]
rs9314932	0.94[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9314933	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9314934	0.89[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506098	0.94[CEU][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506099	0.94[CEU][hapmap];0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506100	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506101	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9506102	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506103	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506105	0.94[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506106	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506107	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506108	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9506110	0.94[CEU][hapmap];0.83[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508268	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508270	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508271	0.94[CEU][hapmap];0.81[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508272	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508278	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9508279	0.89[CEU][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9551600	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9551602	0.94[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9578073	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9579285	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9579286	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9579287	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9579288	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9634353	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv3406145	chr13:29616606-29917459	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29677200-29697800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr13:29680000-29686800	Enhancers	Fetal Heart	heart
3	chr13:29684800-29692200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr13:29685400-29686800	Enhancers	Aorta	Aorta

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