Variant report

Variant	rs61930130
Chromosome Location	chr12:86235691-86235692
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1800832	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55644633	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55694421	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55736533	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55746689	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55754162	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55811116	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55811700	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55853578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55856700	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55899243	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55900789	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55926212	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55966514	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56055322	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56080507	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs56145432	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs56169451	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56208754	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56298026	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs56323012	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61928894	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928895	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928896	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928898	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928900	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928903	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61928904	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61928908	0.97[EUR][1000 genomes]
rs61928913	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61928917	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61928918	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61928956	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61928957	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61928958	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61928959	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930060	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930061	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61930062	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930069	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930070	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61930071	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61930072	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61930073	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930075	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61930079	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61930080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930082	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930122	0.91[EUR][1000 genomes]
rs61930124	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930128	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930131	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61930135	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930136	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61930578	0.83[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs61930583	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs61930594	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61930596	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs61930597	0.84[EUR][1000 genomes]
rs61930598	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs61930627	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs61930642	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61930643	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61930649	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61930651	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61930652	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61930653	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61930863	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930876	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61930878	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930880	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930881	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930882	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61930895	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7132746	0.88[EUR][1000 genomes]
rs7962310	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7973110	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052187	chr12:85954455-86278200	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv541560	chr12:85954455-86278200	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1049179	chr12:86056376-86799188	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1049443	chr12:86185887-86272493	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	n/a
5	esv1797806	chr12:86198935-86425608	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv1036914	chr12:86201703-86272493	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86231000-86237400	Weak transcription	HepG2	liver
2	chr12:86231000-86238800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:86231000-86240400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr12:86235200-86241000	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links