Variant report

Variant	rs4726871
Chromosome Location	chr7:147175913-147175914
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs1018993	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1018994	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1018996	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][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]
rs10251234	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10260316	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10260458	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs10270551	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10276608	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10282026	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10282126	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10952681	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10952682	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10952683	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10952684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs10952685	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11972784	1.00[CEU][hapmap]
rs12540164	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703913	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12703914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1358540	0.95[CEU][hapmap];0.84[CHB][hapmap]
rs1406284	0.88[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1406285	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1468370	0.95[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1528515	1.00[CEU][hapmap];0.87[CHB][hapmap];0.83[EUR][1000 genomes]
rs1528522	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1528527	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1528528	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1528531	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2021879	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2021880	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2022225	1.00[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap]
rs2178212	1.00[CEU][hapmap];0.83[CHB][hapmap];0.84[EUR][1000 genomes]
rs2373132	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2373133	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2373138	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2373139	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2620484	1.00[CEU][hapmap];0.84[CHB][hapmap];0.83[EUR][1000 genomes]
rs2888503	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2888504	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs3915305	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4259337	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4725723	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4725725	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs4725726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4725731	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4725732	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4725735	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4725737	0.95[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4726860	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs4726861	1.00[CEU][hapmap]
rs4726864	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4726870	0.94[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap]
rs4726872	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4726874	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6464803	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs6464804	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs6464805	0.85[CEU][hapmap]
rs6464809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6464810	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6464811	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6464812	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6464813	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6944237	0.95[CEU][hapmap]
rs6947428	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6972045	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs700304	0.80[CEU][hapmap]
rs7781124	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs7782093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7783425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7783548	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7789396	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7794824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7796036	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7805836	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7807007	1.00[CEU][hapmap];0.84[CHB][hapmap]
rs7810880	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs826643	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[EUR][1000 genomes]
rs826644	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs826654	0.81[CEU][hapmap]
rs826791	0.81[CHB][hapmap];0.93[JPT][hapmap]
rs826816	0.81[CEU][hapmap]
rs826831	0.81[CEU][hapmap]
rs917125	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs917126	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147175800-147176200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr7:147175800-147176200	Enhancers	Gastric	stomach

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