Variant report

Variant	rs1427160
Chromosome Location	chr6:48630039-48630040
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1348414	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1427158	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1427159	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1427161	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16877558	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16877594	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16877610	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4596470	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4640885	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56873042	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61092639	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61319711	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6908013	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6915629	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6923183	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6924204	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6926050	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6931059	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73475839	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73475840	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73475846	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73475848	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73475855	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73477824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73479864	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480865	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480867	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480868	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480873	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480875	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480882	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480884	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480887	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480889	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73480891	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480892	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73480901	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73482504	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73482510	1.00[EUR][1000 genomes]
rs73482512	1.00[EUR][1000 genomes]
rs73482514	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73482517	0.86[EUR][1000 genomes]
rs73737126	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv603035	chr6:47902243-48700995	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1033151	chr6:48067287-48797029	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538217	chr6:48067287-48797029	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv830658	chr6:48497904-48632523	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2752125	chr6:48575963-48718589	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv949690	chr6:48595821-49289855	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1034217	chr6:48601590-48714176	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv603036	chr6:48601723-48711041	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
9	nsv1015258	chr6:48607583-48714176	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
10	nsv1024115	chr6:48609036-48648634	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:48627200-48632400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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